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EP1237933A1 - Procede d'oxydation d'alcools primaires - Google Patents

Procede d'oxydation d'alcools primaires

Info

Publication number
EP1237933A1
EP1237933A1 EP00980111A EP00980111A EP1237933A1 EP 1237933 A1 EP1237933 A1 EP 1237933A1 EP 00980111 A EP00980111 A EP 00980111A EP 00980111 A EP00980111 A EP 00980111A EP 1237933 A1 EP1237933 A1 EP 1237933A1
Authority
EP
European Patent Office
Prior art keywords
process according
oxidising
tempo
oxidation
polysaccharide
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP00980111A
Other languages
German (de)
English (en)
Inventor
Susanna Gunnars
Thomas Jaschinski
Petter Bragd
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Essity Nederlands BV
Original Assignee
SCA Hygiene Products Zeist BV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by SCA Hygiene Products Zeist BV filed Critical SCA Hygiene Products Zeist BV
Priority to EP00980111A priority Critical patent/EP1237933A1/fr
Publication of EP1237933A1 publication Critical patent/EP1237933A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B31/00—Preparation of derivatives of starch
    • C08B31/18—Oxidised starch
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H7/00—Compounds containing non-saccharide radicals linked to saccharide radicals by a carbon-to-carbon bond
    • C07H7/02—Acyclic radicals
    • C07H7/033—Uronic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B15/00—Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
    • C08B15/02—Oxycellulose; Hydrocellulose; Cellulosehydrate, e.g. microcrystalline cellulose
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B15/00—Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
    • C08B15/02—Oxycellulose; Hydrocellulose; Cellulosehydrate, e.g. microcrystalline cellulose
    • C08B15/04—Carboxycellulose, e.g. prepared by oxidation with nitrogen dioxide

Definitions

  • the present invention relates to a process of selectively oxidising primary alcohols, in particular primary alcohol functions in monosaccharides and poly- saccharides.
  • Oxidation of primary alcohol functions in molecules to aldehydes and/or carboxylic acids is very useful for introducing functionalities into the molecule, for example for adjusting solubility, reactivity or for providing an anchor for coupling reactions with other molecules.
  • oxidised carbohydrates having an intact carbon skeleton i.e. carbohydrates oxidised at the primary hydroxyl function, are advantageous for certain applications, for example as metal chelating agents, viscosifiers, carrier materials, stabilisers, and superabsorbent polymers.
  • TEMPO 2,2,6,6-tetramethylpiperidinyloxy
  • a two-phase solvent system dichloromethane and water
  • Davis and Flitsch, Tetrahedron Lett. 34, 1181-1184 (1993) reported the oxidation of monosaccharides wherein the non-primary hydroxyl groups are partly protected, using the same oxidation system.
  • the TEMPO oxidations can also be carried out in non-toxic media, especially aqueous media.
  • DE-4209869 discloses the oxidation of alkyl poly- glucosides and other compounds having primary alcohol functions with hypochlorite and TEMPO in aqueous suspension at pH 8-9.
  • De Nooy et al (WO 95/07303 and Reel. Trav. Chim. Pays-Bas 113 (1994) 165-166) have described the oxidation of polysaccharides using TEMPO and a hypohalite in the presence of a catalytic amount of a TEMPO or a related nitroxyl radical in an aqueous reaction medium at a pH of between 9 and 13.
  • DE- 19746805 describes the oxidation of starch with TEMPO, hypochlorite or chlorine, and bromide at pH 7-9.
  • WO 99/23117 and WO 99/23240 describe the oxidation of cellulose and starch, respectively, with TEMPO and an oxidative enzyme (laccase) and oxygen at pH 4-9 resulting in products containing low numbers of carbaldehyde and carboxyl groups.
  • laccase oxidative enzyme
  • TEMPO analogues can be used in the process according to the invention, preference is given to 4-hydroxy-2,2,6,6-tetramethylpiperidin-l-oxyl (4- hydroxy-TEMPO) and acylated derivatives thereof such as 4-acetoxy, 4-phosphonooxy and 4-benzoyloxy-TEMPO, as well as to 4-amino-TEMPO and acylated derivatives thereof such as 4-acetamido- and 4-maleimido-TEMPO. 4-Hydroxy-TEMPO is most preferred.
  • Combinations of nitroxyls can also be used, for example to adjust the aldehyde to acid ratio. A suitable combination is e.g.
  • a precursor is understood to comprise a compound that under the reaction conditions can form nitroxyl radicals, such as the corresponding hydroxyl- amines and nitrones; the di-tert-alkyl nitroxyl may also be prepared for example by oxidation of the corresponding di-tert-alkylamine with hydrogen peroxide and tungstate.
  • a catalytic amount of nitroxyl is preferably 0.05-15 % by weight, based on the dry weight of the primary alcohol, or 0.05-15 mol% with respect to the hydroxymethyl (-CH 2 OH) groups of the molecule, especially the carbohydrate molecule.
  • the nitroxyl is present in an amount of 0.2-5 %.
  • the oxidising agent can be any oxidising agent capable of reoxidising reduced nitroxyls, such as ozone and especially hypohalites. Also hydrogen peroxide or organic hydroperoxides may be used, suitably with a metal catalyst. Furthermore, peracids such as peracetic acid, and perbenzoic acid may be used without the necessity of con- comitantly using halide.
  • the amount of oxidising agent is e.g. 0.1-20 wt.%, especially 0.1-20 wt.%, preferably 0.5-7.5 wt.% with respect to the dry weight of the alcohol.
  • the oxidation can be performed at ambient temperature or increased temperature. The oxidation should be performed at a pH between 2 and 7, especially between 3 and 6 to give best results.
  • the reaction temperature is advantageously kept between 5°C and 50°C.
  • oxidation can be successfully performed without further oxidising agent, especially when 4-acetamido TEMPO or another 4- amido TEMPO or hydroxy-TEMPO is used under acidic conditions.
  • Acidic conditions can be adjusted e.g. by addition of an inert organic or inorganic acid, e.g. sulphuric acid or a sulphonic acid such as toluenesulphonic acid.
  • a lower pH, generally between 0.5 and 3, is used in this embodiment.
  • This embodiment has the advantage that the product is free of any halogen reagent.
  • the actual oxidising species may be the nitroxyl radical, but it may also be a disproportionation product of TEMPO, such as the nitrone.
  • the spent TEMPO derivative can be regenerated off-line, using e.g. ozone or another oxidising agent.
  • the process can be used for introducing low levels of oxidation, it is preferred that at least 10%, more preferably at least 25% of the primary hydroxyl groups are converted to carbaldehyde groups and/or carboxylic groups.
  • the product contains both carbaldehyde groups and carboxylic groups, in a ratio of at least 1 :5, preferably at least 1 :2, up to e.g. 2:1.
  • the process according to the invention can be used for oxidising compounds having primary and or secondary alcohol functions.
  • the process can be used for oxidising compounds having both primary and secondary alcohol functions, such as 1,6-octanediol and, in particular, carbohydrates and their reduced derivatives (glycitols), as the process exhibits a preference of primary over secondary alcohol functions.
  • Both monomeric carbohydrates (monosaccharides), and dimeric, oligomeric and polymeric carbohydrates, as well as sugar alcohols can be oxidised, if they have a primary alcohol function.
  • polymeric carbohydrates examples include ⁇ -glucans, such as cellulose and chitin (1,4- ⁇ ), curdlan and scleroglucan and other 1,3- ⁇ -glucans and fractions, derivatives and hydrolysis products thereof, ⁇ -glucans, in particular starch (1,4- ⁇ ) and pullulan (1,6/1,4/1,4- ⁇ ) and fractions, derivatives and hydrolysis products thereof- such as amylose and maltodextrins-, and cyclic equivalents thereof such as cyclodextrin, also other polysaccharides such as fructans including inulin, and natural or artificial gums such as xanthan (1,4- ⁇ , with side chains), guar, carob flower, algin, gum arabic, dragacanth, agar, ghatti, carrageenin, and the like.
  • ⁇ -glucans such as cellulose and chitin (1,4- ⁇ ), curdlan and scleroglucan and other 1,3- ⁇ -
  • the method is suitable for the oxidation of water- soluble oligosaccharides and polysaccharides such as starch, cellulose, galactomannans and fructans or fractions, hydrolysates or derivatives thereof.
  • polysaccharides are the hydroxyalkyl (hydroxyethyl, hydroxypropyl and the like) derivatives. These can also be oxidised in the side chain, resulting in (additional) formyl- alkyl and or carboxyalkyl derivatives. Carboxyalkyl derivatives such as carboxymethyl cellulose can also be substrates for the present process.
  • the products obtained by the process of the invention are characterised by the presence of carbaldehyde groups and/or carboxyl groups, depending on the reaction conditions (temperature, pH and rate of addition of oxidising agent: more aldehyde at lower temperature, lower pH and slower addition).
  • the aldehyde to acid ratio also depends on the substrate; it is e.g. higher in starch than in short-chain glycosides.
  • the ratio can also be influenced by the nature of the nitroxyl compound; e.g. 4-hydroxy- TEMPO gives a higher ratio than 4-acetamido-TEMPO, and the latter gives a higher ratio than unsubstituted TEMPO.
  • the products can be used as chelating agents for metals and the like.
  • Oxidised polysaccharides according to the invention are also useful as absorbent materials.
  • the products containing carbaldehyde groups are useful starting materials for amino-, imino-, hydroxylamino-functionalised and other derivatives, and as crosslinkable units in e.g. the production of hydrogels and absorbing materials.
  • the carbaldehyde groups can be converted to carboxyl groups by further oxidation, e.g. with alkali metal chlorite.
  • the products can be functionalised further by oxidation, hydroxy- alkylation, carboxymethylation, cationisation, crosslinking with diepoxy or diamino compounds, divinyl sulphone, trimetaphosphates or other reagents.
  • Crosslinking is especially desired for carboxylic products in the production of absorbing polymers, and is preferably performed after the oxidation.
  • the uronic acid content was measured according to the Blumenkrantz assay (Blumenkrantz et al., J. Anal. Biochem. 54, 484 (1973)). About 25 % of the anhydroglucose units were converted in uronic acid groups. However, a significant amount of aldehyde groups was found to be present, which was proven by subsequent oxidation with sodium chlorite. To the still viscous solution 1 gram of sodium chlorite (Aldrich, 80 % purity) was added. A gradual pH increase was observed. By addition of acetic acid the pH was kept below 4. After one day the uronic acid content was measured again and was found to be 35 %.
  • Example 1 The experiment described in Example 1 was repeated using the same amount of starch, but with 400 mg of 4-hydroxy-TEMPO. The pH was kept between 4 and 4.5. In the course of eight hours, 5 ml of sodium hypochlorite solution (2.3 M) was added. According to the Blumenkrantz assay 10 % of the anhydroglucose units were converted into uronic acid. After reaction with sodium chlorite to determine the total degree of primary oxidation, the uronic acid content was increased to 15%. Examples 1 and 2 were not optimised as to total degree of oxidation.
  • Example 3 The experiment described in Example 1 was repeated using the same amount of starch, but now the pH was kept at between 4.8 and 5.0. In the course of six hours sodium hypochlorite was added (0.5 ml per time; in total 15 ml was added). After 18 hours the reaction was finished (no further sodium hydroxide consumption was observed). According to the Blumenkrantz assay 40 % of the anhydroglucose units were converted to uronic acid. By treatment of the reaction product with sodium chlorite/hydrogen peroxide the aldehyde groups present were converted into the acid.
  • Example 5 In 50 ml of water 20 mg of 4-acetoxy TEMPO and 1.1 g of ⁇ -methylglucopyranoside were dissolved. To this solution 3.5 ml of sodium hypochlorite solution (2.3M) was added. During reaction the pH was kept between 5 and 6 by addition of 0.5 M NaOH solution. After completion of the reaction 0.2 ml hydrogen peroxide solution (Merck, 30% w/w) and 400 mg of sodium chlorite (Aldrich) were added. After a small pH increase, the pH dropped from 5 to 4.5. According to the Blumenkrantz method 3.2 mmol of uronic acid was present.
  • Example 7 In 100 ml of water 70 mg of 4-acetamido-TEMPO and 2.04 g of MGP were dissolved. In the course of a few hours portion wise sodium hypochlorite solution was added. To keep the pH at 5 0.5 M sodium hydroxide solution was added. The sodium hydroxide consumption after consumption of 6 ml of sodium hypochlorite was 5.05 mmol. Then, to complete the conversion into carboxylic acid groups 0.20 ml of hydrogen peroxide solution and 0.50 g of sodium chlorite (80%, Aldrich) were added. The reaction mixture was allowed to react for 20 hours. Finally the uronic acid content was measured according to the Blumenkrantz method. The yield was 5.5 mmol., which is in agreement with the amount of sodium hydroxide consumed.
  • the 6-carboxy starch (with a degree of oxidation of 35 %) was dissolved in 18 ml of water , the pH was adjusted to 4.7 and 400 mg of butanediol diglycidyl ether was added. The highly viscous solution was heated at 50 °C during 20 hours. During heating the viscosity increased and finally a gel was obtained.
  • a solution of 400 mg TEMPO and 250 mg of ⁇ -methylglucopyranoside in 80 ml of water was brought to pH 1.17 and then allowed to react for 2 hours. During standing the pH decreased slightly. The final pH value was 1.03. The pH was then brought to 5 and sodium chlorite (150 mg) and hydrogen peroxide (0.10 ml 30 % w/w) were added. After one day the uronic acid content was measured (65 mg, which corresponds to a degree of oxidation of 25%).
  • Example 13 A solution of 0.1 g (0.5 mmol) of ⁇ -methylglucopyranoside and 55 mg of 4-acetamido- TEMPO in 100 ml of water was adjusted to pH 1.5 by addition of concentrated sulphuric acid. The solution was allowed to react for 48 hours at 20°C. The carbonyl content was determined using high performance anionic exchange chromatography (HPAEC) with amperometric detection using DIONEX pulsed electrochemical detector (PED). The primary C6 aldehyde was the only product that was detected. Consequently, no over- oxidation to carboxylates had occurred. The ratio of C aldehyde to unreacted glucopyranoside according to the chromatogram was 0.07 (about 7% conversion).
  • HPAEC high performance anionic exchange chromatography
  • PED DIONEX pulsed electrochemical detector
  • Example 14 Example 13 was repeated, however with a pH adjusted to 0.5. Again, no other product than the C6 aldehyde was detected. The ratio of C aldehyde to unreacted glucopyranoside according to the chromatogram was 0.19 (about 16% conversion).

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Polymers & Plastics (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biotechnology (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Dans un nouveau procédé d'oxydation d'un alcool primaire et/ou d'un alcool secondaire, un agent oxydant est utilisé en présence d'un alkyle nitroxyle bi-tertiaire-, dans un milieu de réaction aqueux à un pH inférieur à 7. L'alkyle nitroxyle bi-tertiaire- est plus spécifiquement du 4-hydroxy-TEMPO, et le procédé est particulièrement avantageux pour oxyder des glucides tels que l'amidon.
EP00980111A 1999-11-08 2000-11-08 Procede d'oxydation d'alcools primaires Withdrawn EP1237933A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP00980111A EP1237933A1 (fr) 1999-11-08 2000-11-08 Procede d'oxydation d'alcools primaires

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP99203726 1999-11-08
EP99203726 1999-11-08
PCT/NL2000/000812 WO2001034657A1 (fr) 1999-11-08 2000-11-08 Procede d'oxydation d'alcools primaires
EP00980111A EP1237933A1 (fr) 1999-11-08 2000-11-08 Procede d'oxydation d'alcools primaires

Publications (1)

Publication Number Publication Date
EP1237933A1 true EP1237933A1 (fr) 2002-09-11

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EP00980111A Withdrawn EP1237933A1 (fr) 1999-11-08 2000-11-08 Procede d'oxydation d'alcools primaires

Country Status (6)

Country Link
US (1) US6770755B1 (fr)
EP (1) EP1237933A1 (fr)
JP (1) JP2003516939A (fr)
AU (1) AU1741101A (fr)
CO (1) CO5231217A1 (fr)
WO (1) WO2001034657A1 (fr)

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WO2001034657A1 (fr) 2001-05-17
US6770755B1 (en) 2004-08-03
CO5231217A1 (es) 2002-12-27
AU1741101A (en) 2001-06-06
JP2003516939A (ja) 2003-05-20

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